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Methylenetetrahydrofolate reductase C677T polymorphism and colorectal cancer susceptibility: a meta-analysis

机译:亚甲基四氢叶酸还原酶C677T多态性与大肠癌易感性的Meta分析

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摘要

The association between methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and colorectal cancer (CRC) susceptibility has been researched in numerous studies. However, the results of these studies were controversial. Therefore, the objective of this meta-analysis was to offer a more convincible conclusion about such association with more included studies. Eligible studies published till May 1, 2017 were searched from PubMed, Embase, Web of Science, and CNKI database about such association. Pooled odds ratios (ORs) together with 95% confidence intervals (CIs) were calculated to evaluate such association. And the Begg’s funnel plot and Egger’s test were applied to assess the publication bias. This meta-analysis contained 37049 cases and 52444 controls from 87 publications with 91 eligible case–control studies. Because of lack of data for a particular genotype in several studies, all the included studies were analysed barely in the dominant model. Originally, there was no association between MTHFR C677T polymorphism and CRC susceptibility (OR =0.99, 95% CI =0.94–1.05). After excluding 13 studies according to their heterogeneity and publication bias, rs1801133 polymorphism was found to reduce the risks of CRC significantly (OR =0.96, 95% CI =0.94–0.99). In the subgroup analysis of ethnicity, there was a significant association in Asians (OR =0.94, 95% CI =0.89–1.00). Furthermore, when stratified by the source of controls and genotyping methods, the positive results were observed in population-based control group (OR =0.97, 95% CI =0.93–1.00) and PCR-restriction fragment length polymorphism (PCR-RFLP) method (OR =0.95, 95% CI =0.91–0.99. The results of the meta-analysis suggested that MTHFR C677T polymorphism was associated with CRC susceptibility, especially in Asian population.
机译:在许多研究中已经研究了亚甲基四氢叶酸还原酶(MTHFR)C677T多态性与结直肠癌(CRC)敏感性之间的关联。但是,这些研究的结果是有争议的。因此,这项荟萃分析的目的是通过更广泛的研究为这种关联提供更令人信服的结论。从PubMed,Embase,Web of Science和CNKI数据库中搜索有关此类关联的发表至2017年5月1日的合格研究。计算合并的优势比(OR)和95%置信区间(CI),以评估这种关联。然后使用Begg的漏斗图和Egger的检验来评估出版偏见。这项荟萃分析包含来自87篇出版物的91项符合条件的病例对照研究的37049例病例和52444例对照。由于在一些研究中缺乏有关特定基因型的数据,因此在优势模型中仅对所有纳入研究进行了分析。最初,MTHFR C677T多态性与CRC敏感性之间没有关联(OR = 0.99,95%CI = 0.94-1.05)。根据异质性和发表偏倚排除了13项研究后,发现rs1801133多态性可显着降低CRC的风险(OR = 0.96,95%CI = 0.94–0.99)。在种族的亚组分析中,亚洲人之间存在显着关联(OR = 0.94,95%CI = 0.89–1.00)。此外,当按对照来源和基因分型方法进行分层时,以人群为基础的对照组(OR = 0.97,95%CI = 0.93–1.00)和PCR限制性片段长度多态性(PCR-RFLP)方法观察到阳性结果(OR = 0.95,95%CI = 0.91-0.99。荟萃分析的结果表明,MTHFR C677T多态性与CRC易感性有关,特别是在亚洲人群中。

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